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Immune Cells Invade the Collateral Circulation during Human Stroke: Prospective Replication and Extension

It remains unclear if principal components of the local cerebral stroke immune response can be reliably and reproducibly observed in patients with acute large-vessel-occlusion (LVO) stroke. We prospectively studied a large independent cohort of n = 318 consecutive LVO stroke patients undergoing mech...

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Autores principales: Strinitz, Marc, Pham, Mirko, März, Alexander G., Feick, Jörn, Weidner, Franziska, Vogt, Marius L., Essig, Fabian, Neugebauer, Hermann, Stoll, Guido, Schuhmann, Michael K., Kollikowski, Alexander M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8430889/
https://www.ncbi.nlm.nih.gov/pubmed/34502070
http://dx.doi.org/10.3390/ijms22179161
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author Strinitz, Marc
Pham, Mirko
März, Alexander G.
Feick, Jörn
Weidner, Franziska
Vogt, Marius L.
Essig, Fabian
Neugebauer, Hermann
Stoll, Guido
Schuhmann, Michael K.
Kollikowski, Alexander M.
author_facet Strinitz, Marc
Pham, Mirko
März, Alexander G.
Feick, Jörn
Weidner, Franziska
Vogt, Marius L.
Essig, Fabian
Neugebauer, Hermann
Stoll, Guido
Schuhmann, Michael K.
Kollikowski, Alexander M.
author_sort Strinitz, Marc
collection PubMed
description It remains unclear if principal components of the local cerebral stroke immune response can be reliably and reproducibly observed in patients with acute large-vessel-occlusion (LVO) stroke. We prospectively studied a large independent cohort of n = 318 consecutive LVO stroke patients undergoing mechanical thrombectomy during which cerebral blood samples from within the occluded anterior circulation and systemic control samples from the ipsilateral cervical internal carotid artery were obtained. An extensive protocol was applied to homogenize the patient cohort and to standardize the procedural steps of endovascular sample collection, sample processing, and laboratory analyses. N = 58 patients met all inclusion criteria. (1) Mean total leukocyte counts were significantly higher within the occluded ischemic cerebral vasculature (I) vs. intraindividual systemic controls (S): +9.6%, I: 8114/µL ± 529 vs. S: 7406/µL ± 468, p = 0.0125. (2) This increase was driven by neutrophils: +12.1%, I: 7197/µL ± 510 vs. S: 6420/µL ± 438, p = 0.0022. Leukocyte influx was associated with (3) reduced retrograde collateral flow (R(2) = 0.09696, p = 0.0373) and (4) greater infarct extent (R(2) = 0.08382, p = 0.032). Despite LVO, leukocytes invade the occluded territory via retrograde collateral pathways early during ischemia, likely compromising cerebral hemodynamics and tissue integrity. This inflammatory response can be reliably observed in human stroke by harvesting immune cells from the occluded cerebral vascular compartment.
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spelling pubmed-84308892021-09-11 Immune Cells Invade the Collateral Circulation during Human Stroke: Prospective Replication and Extension Strinitz, Marc Pham, Mirko März, Alexander G. Feick, Jörn Weidner, Franziska Vogt, Marius L. Essig, Fabian Neugebauer, Hermann Stoll, Guido Schuhmann, Michael K. Kollikowski, Alexander M. Int J Mol Sci Article It remains unclear if principal components of the local cerebral stroke immune response can be reliably and reproducibly observed in patients with acute large-vessel-occlusion (LVO) stroke. We prospectively studied a large independent cohort of n = 318 consecutive LVO stroke patients undergoing mechanical thrombectomy during which cerebral blood samples from within the occluded anterior circulation and systemic control samples from the ipsilateral cervical internal carotid artery were obtained. An extensive protocol was applied to homogenize the patient cohort and to standardize the procedural steps of endovascular sample collection, sample processing, and laboratory analyses. N = 58 patients met all inclusion criteria. (1) Mean total leukocyte counts were significantly higher within the occluded ischemic cerebral vasculature (I) vs. intraindividual systemic controls (S): +9.6%, I: 8114/µL ± 529 vs. S: 7406/µL ± 468, p = 0.0125. (2) This increase was driven by neutrophils: +12.1%, I: 7197/µL ± 510 vs. S: 6420/µL ± 438, p = 0.0022. Leukocyte influx was associated with (3) reduced retrograde collateral flow (R(2) = 0.09696, p = 0.0373) and (4) greater infarct extent (R(2) = 0.08382, p = 0.032). Despite LVO, leukocytes invade the occluded territory via retrograde collateral pathways early during ischemia, likely compromising cerebral hemodynamics and tissue integrity. This inflammatory response can be reliably observed in human stroke by harvesting immune cells from the occluded cerebral vascular compartment. MDPI 2021-08-25 /pmc/articles/PMC8430889/ /pubmed/34502070 http://dx.doi.org/10.3390/ijms22179161 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Strinitz, Marc
Pham, Mirko
März, Alexander G.
Feick, Jörn
Weidner, Franziska
Vogt, Marius L.
Essig, Fabian
Neugebauer, Hermann
Stoll, Guido
Schuhmann, Michael K.
Kollikowski, Alexander M.
Immune Cells Invade the Collateral Circulation during Human Stroke: Prospective Replication and Extension
title Immune Cells Invade the Collateral Circulation during Human Stroke: Prospective Replication and Extension
title_full Immune Cells Invade the Collateral Circulation during Human Stroke: Prospective Replication and Extension
title_fullStr Immune Cells Invade the Collateral Circulation during Human Stroke: Prospective Replication and Extension
title_full_unstemmed Immune Cells Invade the Collateral Circulation during Human Stroke: Prospective Replication and Extension
title_short Immune Cells Invade the Collateral Circulation during Human Stroke: Prospective Replication and Extension
title_sort immune cells invade the collateral circulation during human stroke: prospective replication and extension
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8430889/
https://www.ncbi.nlm.nih.gov/pubmed/34502070
http://dx.doi.org/10.3390/ijms22179161
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